Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 10 for Noonan syndrome 9
  1. SOS1 gene 
    ... function SOS1 mutations cause a distinctive form of Noonan syndrome. Nat Genet. 2007 Jan;39(1):75-9. doi: 10.1038/ng1939. Epub 2006 Dec 13. ...
    https://medlineplus.gov/genetics/gene/sos1 - Genetics
  2. NRAS gene 
    ... M. A restricted spectrum of NRAS mutations causes Noonan syndrome. Nat Genet. 2010 Jan;42(1):27-9. doi: 10.1038/ng.497. Epub 2009 Dec ...
    https://medlineplus.gov/genetics/gene/nras - Genetics
  3. LRP2 gene 
    ... Loscertales M, Robson C, Liu T, MacLaughlin DT, Noonan KM, Russell MK, Walsh ... Nat Genet. 2007 Aug;39(8):957-9. doi: 10.1038/ng2063. Epub 2007 Jul 15. ...
    https://medlineplus.gov/genetics/gene/lrp2 - Genetics
  4. BRAF gene 
    ... Opin Genet Dev. 2007 Feb;17(1):31-9. doi: 10.1016/j.gde.2006.12.005. Citation on PubMed Gelb BD, Tartaglia M. Noonan Syndrome with Multiple Lentigines. 2007 Nov 30 [updated 2022 ...
    https://medlineplus.gov/genetics/gene/braf - Genetics
  5. KRAS gene 
    ... syndrome (described above) and two related disorders called Noonan syndrome and ... and thin.At least nine mutations in the KRAS gene have been reported ...
    https://medlineplus.gov/genetics/gene/kras - Genetics
  6. PTPN11 gene 
    ... 2. Citation on PubMed Tartaglia M, Gelb BD. Noonan syndrome and ... in cancer. J Cell Mol Med. 2015 Sep;19(9):2075-83. doi: 10.1111/jcmm.12618. Epub ...
    https://medlineplus.gov/genetics/gene/ptpn11 - Genetics
  7. MAP2K1 gene 
    ... MAP2K1 cause melorheostosis. Nat Commun. 2018 Apr 11;9(1):1390. doi: ... and Noonan syndromes due to mutations in the RAS/MAPK signalling ...
    https://medlineplus.gov/genetics/gene/map2k1 - Genetics
  8. RIT1 gene 
    ... the RIT1 gene have been found to cause Noonan syndrome. This condition is characterized by mildly unusual facial ... and many other signs and symptoms. People with Noonan syndrome caused by RIT1 gene mutations often have swelling ...
    https://medlineplus.gov/genetics/gene/rit1 - Genetics
  9. DYNC2H1 gene 
    ... also known as Verma-Naumoff syndrome or Saldino-Noonan syndrome. These disorders have signs and symptoms similar to ... retrograde transport protein DYNC2H1 in short-rib polydactyly syndrome. Am J Hum Genet. 2009 Apr;84(4):542-9. doi: 10.1016/j.ajhg.2009.03.015. ...
    https://medlineplus.gov/genetics/gene/dync2h1 - Genetics
  10. LZTR1 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Noonan syndrome More About This Health Condition Mutations in the ...
    https://medlineplus.gov/genetics/gene/lztr1 - Genetics